VEN-O-VAC BLOOD COLLECTION VACUUM TUBES— 510(k) K900856

Substantially Equivalent

Artefactos DE Vidrio S.A. DE C.V.

FDA 510(k) clearance K900856 for VEN-O-VAC BLOOD COLLECTION VACUUM TUBES, Substantially Equivalent on 1990-09-21. Applicant: Artefactos DE Vidrio S.A. DE C.V..

Clearance details

Applicant: Artefactos DE Vidrio S.A. DE C.V.
Product code: Code JKA
Advisory panel: Clinical Chemistry
Date received: 1990-02-23
Decision date: 1990-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mexico, MX

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Adverse events under product code JKA

product code JKA

Injury: 455
Malfunction: 26,686
Other: 4
Total: 27,145

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.